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The lacZ gene identified in this report could be useful in studies involving pathogenic F. tularensis strains that require a native reporter protein.
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The second method involves the use of an introduced (thus non-native) reporter mRNA that provides a real-time, live-cell readout of protein production from translation.
Transgenic genotypes were produced using the proximal GPT for the MBP gene to drive expression of linked, non-native reporter transgenes for HSV-TK and lacZ galactosidase (lacZ; Landry et al., 1998; Xie et al., 2002, 2009).
Transgenic genotypes were produced using the proximal GPT for the MBP gene to drive expression of linked, non-native reporter transgenes for HSV-TK, τ-eGFP (τ-enhanced green fluorescent protein) and/or lacZ (lacZ galactosidase) (Landry et al., 1998; Xie et al., 2002; Jacobs et al., 2007).
In both cases (native and reporter strains) the discrepancy observed between the mRNA and protein levels probably resulted from intrinsic regulatory mechanisms.
Recently a synthetic GUS transgene, codon optimised for use in sugarcane, was shown to generate significantly higher levels of GUS activity than the native GUS reporter gene [ 21].
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To compare these results with previously published data [13], the same test proteins were also fused to the N-terminus of the native topology folding reporter GFP or superfolder GFP.
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